510(k) K181165 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Philips wearable biosensor-G5 Solution
| Applicant | Connected Sensing- A Division of Philips Medical Systems, Cambridge MA, US |
| Decision | Substantially Equivalent, Mar 7, 2019 |
| Received | May 2, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181165
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.